Affiliation:
1. Institute of Molecular Metrology College of Chemistry and Chemical Engineering Qingdao University Qingdao 266071 P. R. China
2. Key Laboratory of Water Security and Water Environment Protection in Plateau Intersection (NWNU) Ministry of Education Key Laboratory of Bioelectrochemistry and Environmental Analysis of Gansu Province College of Chemistry and Chemical Engineering Northwest Normal University Lanzhou 730070 P. R. China
Abstract
AbstractRational design of highly active and stable catalysts for dopamine oxidation is still a great challenge. Herein, inspired by the catalytic pocket of natural enzymes, an iodine (I)‐doped single Fe‐site catalyst (I/FeSANC) is synthesized to mimic the catalytic center of heme enzymes in both geometrical and electronic structures, aiming to enhance dopamine (DA) oxidation. Experimental studies and theoretical calculations show that electronic communication between I and FeN5 effectively modulates the electronic structure of the active site, greatly optimizing the overlap of Fe 3d and O 2p orbitals, thereby enhancing OH adsorption. In addition, the electronic communication induced by iodine doping attenuates the attack of proton hydrogen on the active center, thereby enhancing the stability of I/FeSANC. This work provides new insights into the design of highly active and stable single‐atom catalysts and enhances the understanding of catalytic mechanisms for DA oxidation at the atomic scale.
Funder
National Natural Science Foundation of China
China Postdoctoral Science Foundation
Qingdao Postdoctoral Science Foundation
Natural Science Foundation of Shandong Province